dc.contributor.author |
Nemtarev A.V. |
|
dc.contributor.author |
Nasibullin I.O. |
|
dc.contributor.author |
Fayzullin R.R. |
|
dc.contributor.author |
Grigor'eva L.R. |
|
dc.contributor.author |
Mironov V.F. |
|
dc.date.accessioned |
2021-02-25T20:35:52Z |
|
dc.date.available |
2021-02-25T20:35:52Z |
|
dc.date.issued |
2020 |
|
dc.identifier.issn |
0959-9436 |
|
dc.identifier.uri |
https://dspace.kpfu.ru/xmlui/handle/net/161941 |
|
dc.description.abstract |
© 2020 2,2,2-Trichloro-4-methoxy-1,3,2-benzodioxaphosphole reacts with arylacetylenes or 3-chloropropyne to give 2,7-dichloro-5-methoxy-4-aryl(haloalkyl)-1,2-benzoxaphosphinine 2-oxides. Hydrolysis of the latter leads to the opening of the oxaphosphinine ring and formation of (E)-2-(4-chloro-2- methoxy-6 hydroxyphenyl)ethenylphosphonic acid. |
|
dc.relation.ispartofseries |
Mendeleev Communications |
|
dc.subject |
arylacetylenes |
|
dc.subject |
cascade reactions |
|
dc.subject |
dioxaphospholes |
|
dc.subject |
ethenylphosphonic acids |
|
dc.subject |
oxaphosphinines |
|
dc.subject |
phosphoranes |
|
dc.title |
2,2,2-Trichloro-4-methoxy-1,3,2-benzodioxaphosphole in the reactions with terminal acetylenes |
|
dc.type |
Article |
|
dc.relation.ispartofseries-issue |
1 |
|
dc.relation.ispartofseries-volume |
30 |
|
dc.collection |
Публикации сотрудников КФУ |
|
dc.relation.startpage |
34 |
|
dc.source.id |
SCOPUS09599436-2020-30-1-SID85079838791 |
|